| SKU | Size | Availability | Price | Qty |
|---|---|---|---|---|
| S275398-1mg | 1mg | In stock | $266.90 |
Potent, competitive methyltransferase inhibitor
| Synonyms | sinefungin | 58944-73-3 | ADENOSYL-ORNITHINE | Compound 57926 | Antibiotic A 9145 | Sinefungina | Sinefungine | Sinefunginum | A 9145 | 6,9-Diamino-1-(6-amino-9H-purin-9-yl)-1,5,6,7,8,9-hexadeoxydecofuranuronic acid | 6,9-Diamino-1-(6-amino-9H-purin-9-yl)-1,5,6,7,8,9-hexadeo |
|---|---|
| Specifications & Purity | ≥95% |
| Biochemical and Physiological Mechanisms | Potent, competitive methyltransferase inhibitor (IC 50 values are < 1 and 2.5 μM for PRMT1 abd SET7/9 respectively). Nucleoside S-adenosylmethionine analog. Inhibits RNA synthesis. Shows antibacterial effects. |
| Storage Temp | Store at -20°C,Desiccated |
| Shipped In | Ice chest + Ice pads |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
| Product Description | Sinefungin is a natural nucleoside analog of S-adenosylmethionine and inhibits Streptococcus pneumoniae biofilm growth. Its derivatives can be used as inhibitors and structure probes for human protein lysine methyltransferase SETD2. |
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| Pubchem Sid | 488183684 |
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| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183684 |
| IUPAC Name | (2S,5S)-2,5-diamino-6-[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]hexanoic acid |
| INCHI | InChI=1S/C15H23N7O5/c16-6(1-2-7(17)15(25)26)3-8-10(23)11(24)14(27-8)22-5-21-9-12(18)19-4-20-13(9)22/h4-8,10-11,14,23-24H,1-3,16-17H2,(H,25,26)(H2,18,19,20)/t6-,7-,8+,10+,11+,14+/m0/s1 |
| InChi Key | LMXOHSDXUQEUSF-YECHIGJVSA-N |
| Canonical SMILES | C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CC(CCC(C(=O)O)N)N)O)O)N |
| Isomeric SMILES | C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)C[C@H](CC[C@@H](C(=O)O)N)N)O)O)N |
| WGK Germany | 3 |
| RTECS | HE3140000 |
| PubChem CID | 65482 |
| Molecular Weight | 381.39 |
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| Solubility | Soluble in water |
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| Pictogram(s) | GHS07 |
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| Signal | Warning |
| Hazard Statements | H302:Harmful if swallowed |
| Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
| WGK Germany | 3 |
| RTECS | HE3140000 |
| RIDADR | NONHforallmodesoftransport |
| 1. Wang SY et al.. (2021) Role of epigenetics in unicellular to multicellular transition in Dictyostelium.. Genome Biol, 22 (134). [PMID:33947439] |
| 2. Azizi H et al.. (2017) The Pumilio-domain protein PUF6 contributes to SIDER2 retroposon-mediated mRNA decay in Leishmania.. RNA, 23 (12): (1874-1885). [PMID:28877997] |
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